BridgeBio Pharma, Inc.
MUN:2CL Rapport sur les actions
Capitalisation boursière : €4.6b
BridgeBio Pharma Croissance future
Future contrôle des critères 2/6 BridgeBio Pharma devrait augmenter ses bénéfices et ses revenus de 37.3% et de 41.8% par an respectivement, tandis que le BPA devrait croître de croître de 38.1% par an.
Informations clés
37.3%
Taux de croissance des bénéfices
38.1%
Taux de croissance du BPA
Biotechs croissance des bénéfices 39.3% Taux de croissance des recettes 41.8% Rendement futur des capitaux propres n/a Couverture par les analystes Good
Dernière mise à jour 11 Nov 2024
Mises à jour récentes de la croissance future
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BridgeBio Pharma, Inc. Completes Enrollment of FORTIFY, Phase 3 Registrational Study of BBP-418 in Limb-girdle Muscular Dystrophy Type 2I/R9 (LGMD2I/R9) Oct 01
BridgeBio Pharma, Inc. Presents Additional Data from an Analysis of its Phase 3 ATTRibute-CM and Open-Label Extension Study of Acoramidis in ATTR-CM at the European Society of Cardiology 2024 Aug 31
BridgeBio Pharma, Inc. and QED Therapeutics Announce the Launch of the Initial Phase of MyAchonJourney Aug 19
Second quarter 2024 earnings released: US$0.39 loss per share (vs US$0.98 loss in 2Q 2023) Aug 02 BridgeBio Pharma, Inc. Announces Appointment of Thomas Trimarchi, Ph.D., as President and Chief Operating Officer Jul 23
BridgeBio Pharma, Inc. Surpasses Interim Analysis Enrollment Target and Receives U.S. FDA Rare Pediatric Disease Designation for BBP-418, a Potential Treatment for Limb-Girdle Muscular Dystrophy Type 2I/R9 (LGMD2I/R9) Jun 19
BridgeBio Pharma, Inc. Announces Durable Month 12 and 18 Phase 2 Cohort 5 Results of Oral Infigratinib in Achondroplasia, and First Participant Consented in ACCEL for Hypochondroplasia Jun 05
BridgeBio Pharma Presents Additional Data and Analyses from its Phase 3 ATTRibute-CM Study in Transthyretin Amyloid Cardiomyopathy (ATTR-CM) at ESC-HF, Including That Acoramidis Treatment Significantly Reduced All-Cause Mortality in a Pre-specified Sensitivity Analysis of the Entire Study Population May 14
BridgeBio Pharma, Inc., Annual General Meeting, Jun 21, 2024 Apr 28
BridgeBio Pharma, Inc. Presents Cardiac Magnetic Resonance (CMR) Imaging Evidence Consistent with Clinical Improvement Apr 09 BridgeBio Pharma, Inc. has completed a Follow-on Equity Offering in the amount of $250.00001 million. Mar 07
BridgeBio Pharma, Inc. has completed a Follow-on Equity Offering in the amount of $250.00001 million. Mar 06
BridgeBio Pharma, Inc. has filed a Follow-on Equity Offering. Mar 05
Full year 2023 earnings released: US$3.95 loss per share (vs US$3.26 loss in FY 2022) Feb 23
New major risk - Financial position Feb 22
BridgeBio Pharma, Inc. Announces U.S. Food and Drug Administration Acceptance of New Drug Application for Acoramidis for the Treatment of Patients with Transthyretin Amyloid Cardiomyopathy Feb 06
BridgeBio Pharma, Inc. Shares Positive Results of Single-Arm Phase 3 Study of Acoramidis in Japanese Patients with Transthyretin Amyloid Cardiomyopathy (ATTR-CM) Including No Mortality Reported in the Trial at 30 Months Feb 03
BridgeBio Pharma, Inc. Announces Publication of Positive Results from Phase 3 ATTRibute-CM Study of Acoramidis for Patients with Transthyretin Amyloid Cardiomyopathy in the New England Journal of Medicine Jan 11
BridgeBio Pharma, Inc. Announces First Child Dosed in PROPEL 3, its Phase 3 Clinical Trial for Infigratinib in Children with Achondroplasia Dec 14
BridgeBio Pharma, Inc. Presents Additional Clinical Outcomes Data from the Phase 3 ATTRibute-CM Study of Acoramidis in Patients with Transthyretin Amyloidosis Cardiomyopathy (ATTR-CM) Nov 14
BridgeBio Pharma, Inc. Shares Positive Long-Term Data from an Ongoing Phase 2 Study, Which Support the Potential Use of Glycosylated Alpha-dystroglycan (DG) Levels as a Surrogate Endpoint in Limb-Girdle Muscular Dystrophy Type 2I/R9 Oct 10
BridgeBio Pharma, Inc. announced that it expects to receive $250.003806 million in funding from Qatar Investment Authority and other investors Sep 27 BridgeBio Pharma, Inc. announced that it expects to receive $250.003806 million in funding from Qatar Investment Authority and other investors Sep 26
Bridgebio Pharma Announces Positive Feedback from the U.S. Fda and Eu Ema on the Regulatory Path for A Pivotal Phase 3 Trial of Infigratinib in Children with Achondroplasia Sep 07
BridgeBio Pharma, Inc. Presents Detailed Positive Results from Phase 3 Attribute-CM Study of Acoramidis for Patients with Transthyretin Amyloid Cardiomyopathy (ATTR-CM) At European Society of Cardiology Congress 2023 Aug 28
New minor risk - Financial position Aug 06
Second quarter 2023 earnings released: US$0.98 loss per share (vs US$0.067 loss in 2Q 2022) Aug 04
Bridgebio Pharma Announces Opportunity for Accelerated Approval Pathway in Limb-Girdle Muscular Dystrophy Type 2I (Lgmd2i/R9) Based on Glycosylated Alpha-Dystroglycan (Dg) Levels and Announces First Patient Dosed in Fortify Phase 3 Study Aug 01
Bridgebio Announces Consistently Positive Results from Phase 3 Attribute-Cm Study of Acoramidis for Patients with Transthyretin Amyloid Cardiomyopathy Jul 18
BridgeBio Pharma, Inc. Presents Updated Six Month Results from Its Phase 2 Cohort 5 Trial of Infigratinib in Achondroplasia Jun 21
Full year 2022 earnings released: US$3.26 loss per share (vs US$3.90 loss in FY 2021) Feb 24
Bridgebio Pharma, Inc. Initiates CALIBRATE, A Pivotal Phase 3 Study of Encaleret in Autosomal Dominant Hypocalcemia Type 1 Dec 24
BridgeBio Pharm and ML Bio Solutions Present 12-month Results from Phase 2 Study of BBP-418 in Limb-Girdle Muscular Dystrophy Type 2i (LGMD2i) Oct 15
BridgeBio Pharma, Inc Presents Updated Positive Data from Its BBP-812 Canavan Disease Gene Therapy Program At the 51st Annual Meeting of the Child Neurology Society Oct 14
BridgeBio Pharma Announces First Lung Cancer Patient Dosed in Phase 1/2 Trial and US FDA Fast Track Designation for SHP2 Inhibitor BBP-398 in Combination with Amgen's Lumakras(R) (Sotorasib) Oct 12
BridgeBio Pharma, Inc. to Present New Data on its Novel Approaches to RAS-driven Cancers at the Fourth RAS Initiative Symposium Oct 08
BridgeBio Pharma and Sentynl Therapeutics Receive Marketing Authorization in the EU for NULIBRY® (fosdenopterin) for the Treatment of MoCD Type A Sep 21
BridgeBio Pharma, Inc Announces Dosing of First Patient in Phase 1 Trial of BBP-671 Aug 19
BridgeBio Pharma, Sentynl Therapeutics and Medison Pharma Announce Approval in Israel for NULIBRY® (fosdenopterin) for the Treatment of MoCD Type A Aug 11
BridgeBio Pharma, Inc. Announces Positive Interim Results from PROPEL 2 Jul 28
BridgeBio Pharma, Inc. and Sentynl Therapeutics, Inc. Receive Positive CHMP Opinion for NULIBRY® (Fosdenopterin) for Treatment of MoCD Type A Jul 27
BridgeBio Pharma Announces Positive Phase 1 Data and Phase 2/3 Trial Design for BBP-711, a Potentially Best-In-Class GO Inhibitor for Primary Hyperoxaluria Type 1 (PH1) and Recurrent Kidney Stone Formers Jun 28
BridgeBio Pharma Announces Early Positive Data for BBP-812, its Investigational AAV9 Gene Therapy for Canavan Disease Jun 23
BridgeBio Pharma, Inc. Shares Positive Phase 2B Data and Announces Pivotal Study Design for Phase 3 Trial of Encaleret in Autosomal Dominant Hypocalcemia Type 1 (ADH1) Jun 14
BridgeBio Pharma, Inc. and Venthera, Inc. Presents Preliminary Results from Clinical Trial of VT30 (BBP-681) for Venous, Lymphatic, and Venolymphatic Malformations Jun 11
BridgeBio Pharma Presents Positive Phase 1 Data in Healthy Volunteers, Advancing Development of BBP-671 for Pantothenate Kinase-Associated Neurodegeneration (PKAN) and Organic Acidemias May 28 BridgeBio Pharma, Inc. and Phoenix Tissue Repair, Inc Announce Positive Results from Phase 2 Trial of PTR-01 May 21
BridgeBio Pharma, Inc., Annual General Meeting, Jun 22, 2022 May 02
BridgeBio Pharma Presents Updated Results from Phase 2 Open-label Extension Study of Acoramidis in Transthyretin Amyloid Cardiomyopathy (ATTR-CM) Apr 04
Sentynl Therapeutics Inc. entered into an asset purchase agreement to acquire Global Rights to NULIBRY from BridgeBio Pharma, Inc. (NasdaqGS:BBIO). Mar 10
BridgeBio Pharma Announces Dosing of First Patient in Phase 1/2 Trial of Investigational Gene Therapy for Congenital Adrenal Hyperplasia (CAH) Jan 28
Independent Director recently bought €264k worth of stock Jan 01
Prévisions de croissance des bénéfices et des revenus MUN:2CL - Estimations futures des analystes et données financières antérieures (USD Millions ) Date Recettes Les revenus Flux de trésorerie disponible Cash from Op Moy. Nombre d'analystes 12/31/2026 500 -459 -431 -503 13 12/31/2025 230 -586 -597 -534 18 12/31/2024 331 -400 -375 -422 18 6/30/2024 219 -454 -420 -415 N/A 3/31/2024 219 -538 -606 -603 N/A 12/31/2023 9 -643 -529 -528 N/A 9/30/2023 9 -613 -498 -496 N/A 6/30/2023 6 -573 -488 -486 N/A 3/31/2023 78 -425 -409 -403 N/A 12/31/2022 78 -481 -426 -419 N/A 9/30/2022 89 -491 -468 -460 N/A 6/30/2022 91 -509 -495 -447 N/A 3/31/2022 71 -596 -555 -508 N/A 12/31/2021 70 -563 -546 -498 N/A 9/30/2021 57 -535 -508 -460 N/A 6/30/2021 63 -495 -477 -470 N/A 3/31/2021 9 -520 -472 -467 N/A 12/31/2020 8 -449 -407 -400 N/A 9/30/2020 22 -402 -387 -380 N/A 6/30/2020 41 -346 -305 -298 N/A 3/31/2020 41 -291 -286 -278 N/A 12/31/2019 41 -261 -256 -254 N/A 9/30/2019 27 -226 -228 -224 N/A 6/30/2019 N/A -197 -216 -212 N/A 3/31/2019 N/A -155 -183 -178 N/A 12/31/2018 N/A -131 -155 -137 N/A
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Prévisions de croissance des analystes
Taux de revenus par rapport au taux d'épargne: 2CL devrait rester non rentable au cours des 3 prochaines années.
Bénéfices vs marché: 2CL devrait rester non rentable au cours des 3 prochaines années.
Croissance élevée des bénéfices: 2CL devrait rester non rentable au cours des 3 prochaines années.
Chiffre d'affaires vs marché: Le chiffre d'affaires de 2CL ( 41.8% par an) devrait croître plus rapidement que le marché German ( 5.5% par an).
Croissance élevée des revenus: Le chiffre d'affaires de 2CL ( 41.8% par an) devrait croître plus rapidement que 20% par an.
Prévisions de croissance du bénéfice par action
Rendement futur des capitaux propres
ROE futur: Données insuffisantes pour déterminer si le retour sur capitaux propres de 2CL devrait être élevé dans 3 ans
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